A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6382317



Internal ID9890455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33560668..33562656hg38UCSC Ensembl
chr8:33418186..33420174hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666058
Supporting Variants
SamplesNA20770
Known GenesRNF122
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6382317
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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